Senior Executive-QC

Piramal Pharma Limited; Pithampur; On-site; INR 450,000 - 650,000; Full time

Job summary

Piramal Pharma Solutions is a CDMO offering end-to-end development and manufacturing across the drug lifecycle. Senior Executive-QC will analyze stability samples and finished products, ensuring compliance with GLP/GMP and maintaining documentation to support accurate results.

The role involves operating HPLC, Dissolution, UV spectrophotometry, and Karl Fischer equipment, maintaining incubators and logs, and promptly reporting any deviations to the Head QC.

Qualifications

• Experience with GLP/GMP in a lab setting.
• Proficient in maintaining accurate analytical documentation.
• Knowledge of stability sample analysis and related documentation.

Responsibilities

• Analyze stability samples, finished products, and related documentation per cGMP.
• Maintain stability incubators and chambers and prepare monthly planners.
• Receive/inward/store QC samples and disposition after analysis.
• Concurrently document analytical records and log data in equipment usage logs.
• Provide instant reporting for deviations, OOT, or OOS to Section Head/Head QC.
• Perform additional duties as assigned by section head.

Skills

GLP/GMP awareness

Quality control documentation

Tools

HPLC

Dissolution

UV spectrophotometer

Karl Fischer Apparatus

Job description

Be the First to ApplyDivisionPiramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.For more details, please visit : www.piramalpharmasolutions.comJob TitleSenior Executive-QCJob DescriptionAnalysis and Documentation of samples and maintaining GLP / GMP requirements in lab to achieve correct and accurate results in all analysis.· Analysis of stability sample, finished product, and related documentation as per cGMP.· Responsible for only run the method in the HPLC, Dissolution, UV spectrophotometer and Karl Fisher Apparatus does not access to change the method, report format and method configuration.· Maintenance of stability incubators & chamber.· Preparation of stability monthly planner.· Receipt/Inward/Storage of QC samples and Disposition of sample after analysis.· Concurrent documentation of analytical records and storage of raw data, online entries in Instrument/ Equipment’s usage logbooks.· Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC.· Any additional responsibility assigned by section head.· Maintenance of Bin Card of chemical store.· Implementation of GLP / GMP requirements.· To control and maintain QC Laboratory Records. (Like Laboratory notebook and COA etc.).